Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Endo USA Inc., a Keenova Therapeutics Company
With
Pulse Infoframe
Each participant of the study will have their data collected from the date of confirmed diagnosis of DC to the date of enrollment in the registry, post consent. Data will be collected from the participants clinical records as well as from the participant directly. Data will be collected through Pulse Infoframe's technology platform.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Any adult with a confirmed clinical diagnosis of DC.
Age 18 years (or age of majority in their jurisdiction) or older at time of enrollment.
Willing to participate in the registry (including completion of ePROs) and complete the informed consent form.
Having received DC treatment, either non-surgical or surgical, within 2 weeks before enrollment, at enrollment or any time after the date of enrollment or not having received DC treatment after confirmed diagnosis of DC.
Able to participate in English based registry.
You may not be if
Not having a clinical diagnosis of DC.
Age less than 18 years.
Do not provide informed consent.
Clareo Health | Real-World Data Study to Understand Participant Treatment Outcomes for Dupuytren's Contracture
